24, 1997; 75 FR 16308, Mar. Instructions for Downloading Viewers and Players. The controlled substance law and regulations may be viewed online at: www.nyhealth.gov/professionals/narcotic/. 24, 1971; 36 FR 13386, July 21, 1971, unless otherwise noted. Signup for our newsletter to get notified about sales and new products. ( a) A pharmacist may dispense directly a controlled substance listed in Schedule II that is a prescription drug as determined under section 503 of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. (a) No prescription for a controlled substance listed in Schedule III or IV shall be filled or refilled more than six months after the date on which such prescription was issued. (d) A practitioner may sign a paper prescription in the same manner as he would sign a check or legal document (e.g., J.H. Add any text here or remove it. [68 FR 37410, June 24, 2003, as amended at 75 FR 16308, Mar. 453.410 Dispensing of controlled substances by practitioner. "Director" means the Director of the Division of Consumer Affairs in the Department of Law and Public Safety. . longterm care facilities which are not registered with the DEA shall meet all of the following requirements regarding emergency kits containing controlled substances: (1)The source of supply must be a DEA registered hospital, pharmacy or practitioner. (c) The original and transferred prescription(s) must be maintained for a period of two years from the date of last refill. Sec. Emergency refill of schedule III-V control substances extended to a 30-day supply; a pharmacist may dispense a one-time emergency refill of a 90-day supply for a non-controlled medication (f) A prescription is not required for distribution or dispensing of the substance pursuant to any other Federal, State or local law. A prescription for a controlled substance may only be filled by a pharmacist, acting in the usual course of his professional practice and either registered individually or employed in a registered pharmacy, a registered central fill pharmacy, or registered institutional practitioner. Code E amended Oct. 26, 1972, P.L.1048, No.263) "Controlled substance" means a drug, substance, or immediate precursor included in schedules I through V of this act. The information on this page is current as of Jan 17, 2023. Redesignated at 38 FR 26609, Sept. 24, 1973, as amended at 62 FR 13965, Mar. The pharmacist must notify the nearest office of the Administration if the prescribing individual practitioner fails to deliver a written prescription to him; failure of the pharmacist to do so shall void the authority conferred by this paragraph to dispense without a written prescription of a prescribing individual practitioner. (d) A practitioner may administer or dispense (including prescribe) any Schedule III, IV, or V narcotic drug approved by the Food and Drug Administration specifically for use in maintenance or detoxification treatment to a narcotic dependent person if the practitioner complies with the requirements of 1301.28 of this chapter. (3) In an emergency situation, as described in R 338.3165 of the Michigan Administrative Code, a controlled substance included in schedule 2 may be dispensed on the oral prescription of a practitioner if the prescribing practitioner promptly fills out a prescription form and forwards the prescription form to the dispensing pharmacy within 7 days after the oral prescription is issued. This placement is based upon the substance's medical use, potential for abuse, and safety or dependence liability. Sec. Not more than one day's medication may be administered to the person or for the person's use at one time. 353(b)) only pursuant to a written prescription signed by the practitioner, except as provided in paragraph (d) of this section. (d) All written prescriptions and written records of emergency oral prescriptions shall be kept in accordance with requirements of 1304.04(h) of this chapter. A computer-generated prescription that is printed out or faxed by the practitioner must be manually signed. Prescription information may be provided to an authorized central fill pharmacy by a retail pharmacy for dispensing purposes. (f) As an alternative to the procedures provided by paragraphs (a) through (e) of this section, a computer application may be used for the storage and retrieval of refill information for original paper prescription orders for controlled substances in Schedule III and IV, subject to the following conditions: (1) Any such proposed computerized application must provide online retrieval (via computer monitor or hard-copy printout) of original prescription order information for those prescription orders that are currently authorized for refilling. No later than the close of business on the next business day after dispensing a controlled substance . These are also valid for 180 days or up to five refills. 1306.27 Provision of prescription information between retail pharmacies and central fill pharmacies for initial and refill prescriptions of Schedule III, IV, or V controlled substances. Section 3719.01 of the Ohio Revised Code defines an "opioid analgesic" as a controlled substance . (c) The following information must be retrievable by the prescription number: (1) The name and dosage form of the controlled substance. (vi) Name of pharmacist who transferred the prescription. . (1) dispense or deliver a controlled substance or cause a controlled substance to be dispensed or delivered under the pharmacist's direction or supervision except under a valid prescription and in the course of professional practice; (b) An individual practitioner may administer or dispense directly a controlled substance listed in Schedule III, IV, or V in the course of his/her professional practice without a prescription, subject to 1306.07. (4) The initials of the dispensing pharmacist for each refill. (c) A prescription may not be issued for "detoxification treatment" or "maintenance treatment," unless the prescription is for a Schedule III, IV, or V narcotic drug approved by the Food and Drug Administration specifically for use in maintenance or detoxification treatment and the practitioner is in compliance with requirements in 1301.28 of this chapter. 893.049(1)(d), (e),f.s. 24, 1971. (c) Any online pharmacy that participates in the transfer between pharmacies of prescription information must do so in accordance with the requirements of 1306.15 and 1306.25 of this part. The quantity of Schedule III, IV or V controlled substances prescribed or dispensed at any one time shall be limited to a ninety-day supply . For example, this would include a refill-by-refill audit trail for any specified strength and dosage form of any controlled substance (by either brand or generic name or both). Controlled Substances in Schedules III-V may always be prescribed by oral prescription under 21 U.S.C. 24, 1997]. A corresponding liability rests upon the pharmacist, including a pharmacist employed by a central fill pharmacy, who fills a prescription not prepared in the form prescribed by DEA regulations. Prescriptions for controlled substances are limited to a 30-day supply. In lieu of such a printout, the pharmacy shall maintain a bound log book, or separate file, in which each individual pharmacist involved in such dispensing shall sign a statement (in the manner previously described) each day, attesting to the fact that the refill information entered into the computer that day has been reviewed by him and is correct as shown. The new Public Health Law that went into full effect on April 19, 2006 made no changes to the requirements for electronic prescribing. 21 USC 829(a), 21 CFR 1306.12(a). (d) If the pharmacist merely initials and dates the back of the prescription or annotates the electronic prescription record, it shall be deemed that the full face amount of the prescription has been dispensed. If such an application provides a hard-copy printout of each day's controlled substance prescription order refill data, that printout shall be verified, dated, and signed by the individual pharmacist who refilled such a prescription order. (c) To annotate an electronic prescription, a pharmacist must include all of the information that this part requires in the prescription record. More information can be found in Title 21 United States Code (USC) Controlled Substances Act. (a) The transfer of original prescription information for a controlled substance listed in Schedule III, IV, or V for the purpose of refill dispensing is permissible between pharmacies on a one-time basis only. (a) A prescription for a controlled substance to be effective must be issued for a legitimate medical purpose by an individual practitioner acting in the usual course of his professional practice. CHAPTER 315. Practitioners are required to review a patient's controlled substance prescription history and opioid antidote administration history, pursuant to Section 44-130-60 or 44-130-80, before issuing a prescription for a Schedule II controlled substance in accordance with Section 44-53-1645 (A). Note: If you need help accessing information in different file formats, see Schedule IV and V drugs can be faxed and given orally. 823(g)); and. Under parameters established by the New York State Board of Pharmacy, prescriptions for non-controlled substances may continue to be electronically transmitted to the pharmacy, either: Both transmissions are considered electronic prescribing, therefore it is The facsimile serves as the original written prescription for purposes of this paragraph (f) and it shall be maintained in accordance with 1304.04(h). Section 80.67 - Schedule II and certain other substances. This webpage will outline the various policies and laws the state of Tennessee have implemented. Electronic Code of Federal Regulations (eCFR). The pharmacy must receive the written prescription within 7 days, and it must state on the face "Authorization for Emergency Dispensing" with the date of the oral order. The Controlled Substances Act and DEA's implementing regulations prohibit the refilling of schedule II controlled substances. (b) The central fill pharmacy receiving the transmitted prescription must: (1) Keep a copy of the prescription (if sent via facsimile) or an electronic record of all the information transmitted by the retail pharmacy, including the name, address, and DEA registration number of the retail pharmacy transmitting the prescription; (2) Keep a record of the date of receipt of the transmitted prescription, the name of the pharmacist filling the prescription, and the date of filling of the prescription; (3) Keep a record of the date the filled prescription was delivered to the retail pharmacy and the method of delivery (i.e.
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